METRONIDazole Injection, USP 500 mg (5 mg/mL) in 100 mL Single Dose Flexible Container, Rx only, For IV Use, Hospira Inc., Lake Forest, IL --- NDC 0409-7811-24

Recall Number: D-0480-2017

Firm: Hospira Inc., A Pfizer Company

Classification: Class II

Status: Terminated

Report Date: 20170301

Initiation Date: 20170210

Termination Date: 20190403

Reason for Recall

Lack of Sterility Assurance: customer report of leaking bag

Product Description

METRONIDazole Injection, USP 500 mg (5 mg/mL) in 100 mL Single Dose Flexible Container, Rx only, For IV Use, Hospira Inc., Lake Forest, IL --- NDC 0409-7811-24